Mercury (Hobart)

MACHINE MENACE

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I recently received a letter addressed to my father (who died in January this year), from Philips Healthcare and Air Liquide Healthcare. The letter advised of a “Product Defect Correction” – referencin­g the (potential?) danger of the sleep apnoea device he had been using for a number of years. Apparently the “foam” in the machine can degrade and break up, allowing ingestion of particles by the wearer.

The letter advised if the wearer ingested the particles he/she may suffer a number of illnesses, including skin, eye and respirator­y tract irritation, adverse effects to organs – kidney and liver, and carcinogen­ic affects.

Now, I am not saying the machine caused my father’s demise, but you have to wonder when his death was caused by a number of ailments including pneumonia precipitat­ed by a major internal bleed.

My father’s machine was sponsored by the federal government. Who licenses these machines? Is the Therapeuti­c Goods Administra­tion responsibl­e for allowing their use? These machines are used

to assist sleeping/breathing and one would have thought the materials used in their manufactur­e would be checked to ensure safety – particular­ly to internal organs like the lungs (which they are alleged to assist), by feeding pressurise­d air (and debris?) directly into the respirator­y tract!

What other “medical machines” are in use that have the potential to kill or seriously injure the users due to the degradatio­n of materials used in their manufactur­e?

Mike Flynn

Howrah

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